Variant #0000324346 (NC_000016.9:g.188346_188377del, NC_000016.9(NM_001077350.2):c.-67-2_-38del (NPRL3))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.188346_188377del
DNA change (hg38) g.138347_138378del
Published as NPRL3(NM_001039476.2):c.-401_-370del (p.(=))
ISCN -
DB-ID NPRL3_000004
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-07 11:05:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPG NM_001015052.2 ?/. - c.*52570_*52601del r.(=) p.(=)
NPRL3 NM_001077350.2 ?/. - c.-67-2_-38del r.spl? p.?
HBZ NM_005332.2 ?/. - c.-14563_-14532del r.(?) p.(=)


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